A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3590111



Internal ID6977439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:26153217..26156000hg38UCSC Ensembl
Innerchr2:26153219..26155998hg38UCSC Ensembl
Outerchr2:26153215..26156002hg38UCSC Ensembl
chr2:26376086..26378869hg19UCSC Ensembl
Innerchr2:26376088..26378867hg19UCSC Ensembl
Outerchr2:26376084..26378871hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg382784
hg192784
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10433262, essv10433261, essv10433303, essv10433287, essv10433283, essv10433282, essv10433309, essv10433276, essv10433332, essv10433316, essv10433284, essv10433292, essv10433277, essv10433321, essv10433274, essv10433329, essv10433280, essv10433267, essv10433297, essv10433288, essv10433304, essv10433298, essv10433312, essv10433311, essv10433323, essv10433296, essv10433328, essv10433310, essv10433290, essv10433314, essv10433294, essv10433260, essv10433271, essv10433318, essv10433268, essv10433307, essv10433299, essv10433265, essv10433281, essv10433308, essv10433302, essv10433295, essv10433289, essv10433269, essv10433317, essv10433293, essv10433285, essv10433313, essv10433266, essv10433330, essv10433272, essv10433264, essv10433326, essv10433286, essv10433275, essv10433273, essv10433279, essv10433291, essv10433327, essv10433300, essv10433263, essv10433320, essv10433319, essv10433324, essv10433305, essv10433315, essv10433306, essv10433278, essv10433322, essv10433331, essv10433301, essv10433325, essv10433270
SamplesNA20339, HG02628, NA19204, NA18861, HG03163, NA19378, HG03247, HG02891, HG03280, NA18510, NA19379, NA19319, NA19119, NA19023, HG02816, HG01242, HG02981, NA19404, NA18868, NA19317, NA19239, HG03267, HG03073, NA19456, HG02715, NA19027, HG02716, HG03343, HG03120, HG03363, NA19455, NA19043, HG02976, NA19118, NA19042, HG03388, HG01241, NA19320, NA20282, HG03046, HG02256, HG02568, HG01956, NA19436, NA20296, HG02813, NA19309, NA19147, NA19712, NA19434, HG02501, NA19144, HG02314, HG03259, NA19439, HG03473, HG02558, NA19376, HG03157, NA19472, HG02646, HG03063, HG03258, HG03410, HG02013, NA19030, HG03445, NA19430, NA19312, NA18511, HG03303, HG03439, HG03166
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3590111
Frequency
Sample Size2504
Observed Gain0
Observed Loss73
Observed Complex0
Frequencyn/a


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